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lignoceric acid  (Tokyo Chemical Industry)

 
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    Tokyo Chemical Industry lignoceric acid
    Lignoceric Acid, supplied by Tokyo Chemical Industry, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lignoceric+acid/acid+lignoceric/us12544831-132-29-33
    Average 86 stars, based on 1 article reviews
    lignoceric acid - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Droplet Countercurrent Chromatography:

    Article Title: Photoactivatable Materials for Versatile Single-Cell Patterning Based on the Photocaging of Cell-Anchoring Moieties through Lipid Self-Assembly
    Article Snippet: Boc-Lys-OH was from Watanabe Chemical Industries, Ltd. (Hiroshima, Japan). .. NSuccinimidyl acetate, octanoic acid, lauric acid, pentadecanoic acid, stearic acid, lignoceric acid, trifluoroacetic acid (TFA), N,N'-dicyclohexylcarbodiimide (DCC), 4-nitrophenyl cholroformate, Nhydroxysuccinimide (NHS), and (1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (WSC) were from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan). .. Triethylamine (Et3N), anhydrous dichloromethane (DCM), anhydrous N,N-dimethylformamide (DMF), diethyl ether, tetrahydrofuran dehydrated stabilizer-free (THF), and deuterated chloroform (CDCl3) were from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

    Produced:

    Article Title: Dust core
    Article Snippet: .. A magnetic nanoparticle compact (dust core pellet (outer diameter 3 mmφ)) was made in the same manner as in Example 1 except that 0.025 g (0.5% by mass) of lignoceric acid (produced by Tokyo Chemical Industry Co., Ltd.), which was saturated aliphatic carboxylic acid, was used in place of gallic acid, and the density of the compact was calculated. ..

    other:

    Article Title: Synergistic effect of very long-chain fatty acid and α-linolenic acid treatments on enteric methane mitigation in the rumen
    Article Snippet: Individual fatty acids, including behenic acid (C22:0, > 95.0%), lignoceric acid (C24:0, > 96.0%), and α-linolenic acid (ALA, C18:3n3, > 70.0%), were purchased from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan).

    Molecular Weight:

    Article Title: Manufacturing method of electronic device
    Article Snippet: —Monocarboxylic Acid— Abietic acid (manufactured by Tokyo Chemical Industry Co., Ltd.) Isopimaric acid (manufactured by Sigma-Aldrich Co., LLC.) .. Lignoceric acid (manufactured by Tokyo Chemical Industry Co., Ltd.) —Dicarboxylic Acid— Succinic acid (manufactured by FUJIFILM Wako Pure Chemical Corporation) Glutaric acid (manufactured by FUJIFILM Wako Pure Chemical Corporation) —Other Carboxylic Acids— Polyacrylic acid (manufactured by FUJIFILM Wako Pure Chemical Corporation, weight-average molecular weight: 5000) —Solvent— Isopropanol (manufactured by FUJIFILM Wako Pure Chemical Corporation) Methyl ethyl ketone (manufactured by FUJIFILM Wako Pure Chemical Corporation) TABLE 1 Molecular Treatment Treatment Treatment Treatment Treatment Treatment Treatment weight liquid 1 liquid 2 liquid 3 liquid 4 liquid 5 liquid 6 liquid 7 Monocarboxylic Abietic acid 302.45 10 7 — — 8 — — acid Isopimaric 302.45 — 3 — — — — — acid Dicarboxylic Succinic acid 118.09 — — 10 — 2 — — acid Glutaric acid 132.12 — — — 10 — — — Other Lignoceric 368.63 — — — — — 10 — carboxylic acids acid Polyacrylic — — — — — — 10 acid Solvent Isopropanol 90 70 90 80 50 20 50 Methyl — 20 — 10 40 70 40 ethyl ketone ..

    Solvent:

    Article Title: Manufacturing method of electronic device
    Article Snippet: —Monocarboxylic Acid— Abietic acid (manufactured by Tokyo Chemical Industry Co., Ltd.) Isopimaric acid (manufactured by Sigma-Aldrich Co., LLC.) .. Lignoceric acid (manufactured by Tokyo Chemical Industry Co., Ltd.) —Dicarboxylic Acid— Succinic acid (manufactured by FUJIFILM Wako Pure Chemical Corporation) Glutaric acid (manufactured by FUJIFILM Wako Pure Chemical Corporation) —Other Carboxylic Acids— Polyacrylic acid (manufactured by FUJIFILM Wako Pure Chemical Corporation, weight-average molecular weight: 5000) —Solvent— Isopropanol (manufactured by FUJIFILM Wako Pure Chemical Corporation) Methyl ethyl ketone (manufactured by FUJIFILM Wako Pure Chemical Corporation) TABLE 1 Molecular Treatment Treatment Treatment Treatment Treatment Treatment Treatment weight liquid 1 liquid 2 liquid 3 liquid 4 liquid 5 liquid 6 liquid 7 Monocarboxylic Abietic acid 302.45 10 7 — — 8 — — acid Isopimaric 302.45 — 3 — — — — — acid Dicarboxylic Succinic acid 118.09 — — 10 — 2 — — acid Glutaric acid 132.12 — — — 10 — — — Other Lignoceric 368.63 — — — — — 10 — carboxylic acids acid Polyacrylic — — — — — — 10 acid Solvent Isopropanol 90 70 90 80 50 20 50 Methyl — 20 — 10 40 70 40 ethyl ketone ..



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    Image Search Results


    A Schematic created using BioRender illustrating PISD enzyme reaction with phosphatidylserine (PS) to form CO 2 and phosphatidylethanolamine (PE). B Schematic created using BioRender showing generation of shScrambled (shSCR) and shPISD lentivirus in 293T cells and subsequent infection and gene silencing in HEPA1-6 cells. C The shPISD lentivirus reduced PISD mRNA abundance ( n = 2 per group) and altered the abundance of various genes involved in phospholipid metabolism ( n = 5 per group). D PISD activity was reduced in shPISD treated cells ( n = 3 per group). E , F Thin layer chromatography images indicating shPISD treated cells had reduced mitochondrial PE content ( E ) and densitometry quantification of thin layer chromatography images presented in E ( n = 3 per group) ( F ). G A Seahorse mitochondrial stress test reveals shPISD treated cells have reduced FCCP stimulated respiration rates ( n = 10 per group). H shPISD treated cells have elevated proton leak, calculated by subtracting oxygen consumption rates (OCR) during basal conditions from OCR during oligomycin (oligo) treated conditions ( n = 10 per group). I , J Western blot image indicating shPISD treated cells have reduced complex I and IV protein abundance ( I ) and densitometry quantification of Western blot images shown in I ( n = 6 per group) ( J ). K 1- 14 C oleate oxidation is reduced in shPISD treated cells ( n = 6 per group). L 1- 14 C lignoceric acid oxidation is increased in shPISD treated cells ( n = 6 per group). M PCA plot of untargeted metabolomics data illustrating that shPISD treated cells have an altered metabolome compared to shSCR treated cells ( n = 3 per group). N Volcano plot of untargeted metabolomics data illustrating differences in metabolites between shSCR and shPISD treated cells ( n = 3 per group). O Heatmap of select lipid metabolism related metabolites that were differentially expressed between shSCR and shPISD treated cells ( n = 3 per group). The data are presented as means ± S.D.

    Journal: Oncogenesis

    Article Title: Targeting mitochondrial phosphatidylethanolamine alters mitochondrial metabolism and proliferation in hepatocellular carcinoma

    doi: 10.1038/s41389-025-00593-y

    Figure Lengend Snippet: A Schematic created using BioRender illustrating PISD enzyme reaction with phosphatidylserine (PS) to form CO 2 and phosphatidylethanolamine (PE). B Schematic created using BioRender showing generation of shScrambled (shSCR) and shPISD lentivirus in 293T cells and subsequent infection and gene silencing in HEPA1-6 cells. C The shPISD lentivirus reduced PISD mRNA abundance ( n = 2 per group) and altered the abundance of various genes involved in phospholipid metabolism ( n = 5 per group). D PISD activity was reduced in shPISD treated cells ( n = 3 per group). E , F Thin layer chromatography images indicating shPISD treated cells had reduced mitochondrial PE content ( E ) and densitometry quantification of thin layer chromatography images presented in E ( n = 3 per group) ( F ). G A Seahorse mitochondrial stress test reveals shPISD treated cells have reduced FCCP stimulated respiration rates ( n = 10 per group). H shPISD treated cells have elevated proton leak, calculated by subtracting oxygen consumption rates (OCR) during basal conditions from OCR during oligomycin (oligo) treated conditions ( n = 10 per group). I , J Western blot image indicating shPISD treated cells have reduced complex I and IV protein abundance ( I ) and densitometry quantification of Western blot images shown in I ( n = 6 per group) ( J ). K 1- 14 C oleate oxidation is reduced in shPISD treated cells ( n = 6 per group). L 1- 14 C lignoceric acid oxidation is increased in shPISD treated cells ( n = 6 per group). M PCA plot of untargeted metabolomics data illustrating that shPISD treated cells have an altered metabolome compared to shSCR treated cells ( n = 3 per group). N Volcano plot of untargeted metabolomics data illustrating differences in metabolites between shSCR and shPISD treated cells ( n = 3 per group). O Heatmap of select lipid metabolism related metabolites that were differentially expressed between shSCR and shPISD treated cells ( n = 3 per group). The data are presented as means ± S.D.

    Article Snippet: 1- 14 C Lignoceric Acid was purchased from American Radiolabeled Chemicals (ARC-0805-50, Saint Louis, MO, USA).

    Techniques: Infection, Activity Assay, Thin Layer Chromatography, Western Blot, Quantitative Proteomics